Acid Oligomers Research Articles

Polar Constituents of Salvia willeana (Holmboe) Hedge, Growing Wild in Cyprus.

Twenty compounds were isolated from the aerial parts of Salvia willeana (Holmboe) Hedge, growing wild in Cyprus. These compounds comprise one new and one known acetophenone, one megastigmane glucoside, five phenolic derivatives, two caffeic acid oligomers, three flavonoids, two lignans, two triterpene acids, one monoterpene glucoside, and two fatty acids. The structures of the isolated compounds were established by means of NMR [(Rotating-frame OverhauserEffect SpectroscopY) (1H-1H-COSY (COrrelation SpectroscopΥ), 1H-13C-HSQC (Heteronuclear Single Quantum Correlation), HMBC (Heteronuclear Multiple Bond Correlation), NOESY (Nuclear Overhauser Effect SpectroscopY), ROESY (Rotating-frame Overhauser Effect SpectroscopY)] and MS spectral analyses. This is the first report of the natural occurrence of 4-hydroxy-acetophenone 4-O-(3,5-dimethoxy-4-hydroxybenzoyl)-β-d-glucopyranoside. A chemical review on the non-volatile secondary metabolites has been carried out. Based on the literature data, the analysis revealed that the chemical profile of S. willeana is close to that of S. officinalis L.

Size-Dependent Affinity of Glycine and Its Short Oligomers to Pyrite Surface: A Model for Prebiotic Accumulation of Amino Acid Oligomers on a Mineral Surface.

The interaction strength of progressively longer oligomers of glycine, (Gly), di-Gly, tri-Gly, and penta-Gly, with a natural pyrite surface was directly measured using the force mode of an atomic force microscope (AFM). In recent years, selective activation of abiotically formed amino acids on mineral surfaces, especially that of pyrite, has been proposed as an important step in many origins of life scenarios. To investigate such notions, we used AFM-based force measurements to probe possible non-covalent interactions between pyrite and amino acids, starting from the simplest amino acid, Gly. Although Gly itself interacted with the pyrite surface only weakly, progressively larger unbinding forces and binding frequencies were obtained using oligomers from di-Gly to penta-Gly. In addition to an expected increase of the configurational entropy and size-dependent van der Waals force, the increasing number of polar peptide bonds, among others, may be responsible for this observation. The effect of chain length was also investigated by performing similar experiments using l-lysine vs. poly-l-lysine (PLL), and l-glutamic acid vs. poly-l-glutamic acid. The results suggest that longer oligomers/polymers of amino acids can be preferentially adsorbed on pyrite surfaces.

Aptamer-based lateral flow assays

Lateral flow assays as point-of-care devices have attracted interest due to their advantages including low costs, easy operation by non-specialized users and low analyte volumes needed. These advantages make lateral flow assays to superior tools for the on-site detection of analytes with qualitative or semi-quantitative results within minutes. Aptamers are single-stranded nucleic acid oligomers with distinct conformational shapes that can bind their corresponding targets via molecular recognition. Due to their specific properties like an efficient chemical synthesis, a longer shelf life and easy introduction of modifications aptamers seem to be ideal biological recognition elements. Moreover, they enable the design of intelligent detection schemes not available with antibodies. This review focuses on lateral flow assays utilizing aptamers as an element for molecular recognition. In the first part of the review, a brief overview on lateral flow assays and aptamers, regarding their generation and properties, will be given. In the second part, a review of recently published literature on this topic will demonstrate the broad spectrum of possible applications and analytes, detectable with aptamer-based lateral flow assays.

Antiviral Agents Against Ebola Virus Infection: Repositioning Old Drugs and Finding Novel Small Molecules.

Ebola virus (EBOV) causes a deadly hemorrhagic syndrome in humans with mortality rate up to 90%. First reported in Zaire in 1976, EBOV outbreaks showed a fluctuating trend during time and fora long period it was considered a tragic disease confined to the isolated regions of the African continent where the EBOV fear was perpetuated among the poor communities. The extreme severity of the recent 2014–16 EBOV outbreak in terms of fatality rate and rapid spread out of Africa led to the understanding that EBOV is a global health risk and highlights the necessity to find countermeasures against it. In the recent years, several small molecules have been shown to display in vitro and in vivo efficacy against EBOV and some of them have advanced into clinical trials. In addition, also existing drugs have been tested for their anti-EBOV activity and were shown to be promising candidates. However, despite the constant effort addressed to identify anti-EBOV therapeutics, no approved drugs are available against EBOV yet.In this chapter, we describe the main EBOV life cycle steps, providing a detailed picture of the druggable viral and host targets that have been explored so far by different technologies. We then summarize the small molecules, nucleic acid oligomers, and antibody-based therapies reported to have an effect either in in silico, or in biochemical and cell-based assays or in animal models and clinical trials, listing them according to their demonstrated or putative mechanism of action.

Design and Preparation of Highly Filled Water‐Borne Polymer–Gibbsite Nanocomposites

AbstractHighly filled, high solids content, water‐borne polymer–Gibbsite nanocomposites are prepared with Gibbsite contents as high as 35 wt%. The polymer–Gibbsite nanocomposites are synthesised via conventional starved feed emulsion polymerization using negatively charged butyl acrylate‐co‐acrylic acid oligomers, which functioned as electrosteric stabilizers for the initial platelets and the subsequently formed latex particles. A simple mathematical model describing the amount of cooligomer required for the colloidal stability of the initial Gibbsite platelets and the subsequently formed particles was derived. This model was used to determine the reaction conditions required for obtaining colloidally stable nanocomposites with a targeted filler content. Cryogenic transmission electron microscopy characterization of the resulting nanocomposites with filler contents up to 20 wt% revealed fully encapsulated Gibbsite platelets and a mixed morphology of “muffin‐like” and encapsulated particles was obtained at higher filler contents.

Adsorption of Methylene Blue and Metanil Yellow Dyes by Modified Carbon Sorbents

Adsorption properties of carbon sorbents modified with glycolic and lactic acid oligomers and copolymers of these toward organic dyes of varied nature: Methylene Blue and Metanil Yellow were studied. Differences in the adsorption of the dyes by the modified sorbents, due to the nature of their surface, were found.

Reductive Dechlorination of Hexachlorobutadiene by a Pd/Fe Microparticle Suspension in Dissolved Lactic Acid Polymers: Degradation Mechanism and Kinetics

Reductive dechlorination of hexachlorobutadiene (HCBD) was performed by a suspension of scattered spots of palladium nanoparticles deposited on iron microparticles (nPd/μZVI) in a mixture of dissolved lactic acid polymers and oligomers (referred to as PLA). The effects of nPd/μZVI loading, temperature, HCBD initial concentration, and PLA content were investigated as to define the best conditions for the dechlorination. HCBD dechlorination by nPd/μZVI occurred in a two-step process: first, HCBD adsorbed onto the nPd surface, which resulted in a rapid initial disappearance of pollutant in solution, and, second, it degraded chemically by atomic hydrogen H*, which resulted from the dissociative adsorption of H2 on nPd. HCBD remained adsorbed on the surface until its complete degradation in nonchlorinated product, in agreement with the formation of an ordered activated complex on the nPd/μZVI surface as suggested by the negative entropy of activation calculated from the Eyring equation. Hence, a minimum amount of nPd/μZVI was required to enable simultaneously HCBD adsorption and H2 production. In these cases, pseudo-first order rate equations were suitable to model HCBD disappearance kinetics. The increase in PLA content resulted in enhancing initial pH decrease such as to maintain acidic conditions and thus high reactivity over a longer period of time. It also resulted in enhancing the contact between HCBD and nPd/μZVI, which was characterized by a more important initial adsorption. As a consequence, deviations from pseudo-first order kinetics were observed and a more representative model with a two-phase decay was proposed.

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids.

RNAs are emerging as important biomarkers and therapeutic targets. Thus, there is great potential in developing chemical probes and therapeutic ligands for the recognition of RNA sequence and structure. Chemically modified Peptide Nucleic Acid (PNA) oligomers have been recently developed that can recognize RNA duplexes in a sequence-specific manner. PNAs are chemically stable with a neutral peptide-like backbone. PNAs can be synthesized relatively easily by the manual Boc-chemistry solid-phase peptide synthesis method. PNAs are purified by reverse-phase HPLC, followed by molecular weight characterization by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF). Non-denaturing polyacrylamide gel electrophoresis (PAGE) technique facilitates the imaging of the triplex formation, because carefully designed free RNA duplex constructs and PNA bound triplexes often show different migration rates. Non-denaturing PAGE with ethidium bromide post staining is often an easy and informative technique for characterizing the binding affinities and specificities of PNA oligomers. Typically, multiple RNA hairpins or duplexes with single base pair mutations can be used to characterize PNA binding properties, such as binding affinities and specificities. 2-Aminopurine is an isomer of adenine (6-aminopurine); the 2-aminopurine fluorescence intensity is sensitive to local structural environment changes, and is suitable for the monitoring of triplex formation with the 2-aminopurine residue incorporated near the PNA binding site. 2-Aminopurine fluorescence titration can also be used to confirm the binding selectivity of modified PNAs towards targeted double-stranded RNAs (dsRNAs) over single-stranded RNAs (ssRNAs). UV-absorbance-detected thermal melting experiments allow the measurement of the thermal stability of PNA-RNA duplexes and PNA·RNA2 triplexes. Here, we describe the synthesis and purification of PNA oligomers incorporating modified residues, and describe biochemical and biophysical methods for characterization of the recognition of RNA duplexes by the modified PNAs.

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids

RNAs are emerging as important biomarkers and therapeutic targets. Thus, there is great potential in developing chemical probes and therapeutic ligands for the recognition of RNA sequence and structure. Chemically modified Peptide Nucleic Acid (PNA) oligomers have been recently developed that can recognize RNA duplexes in a sequence-specific manner. PNAs are chemically stable with a neutral peptide-like backbone. PNAs can be synthesized relatively easily by the manual Boc-chemistry solid-phase peptide synthesis method. PNAs are purified by reverse-phase HPLC, followed by molecular weight characterization by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF). Non-denaturing polyacrylamide gel electrophoresis (PAGE) technique facilitates the imaging of the triplex formation, because carefully designed free RNA duplex constructs and PNA bound triplexes often show different migration rates. Non-denaturing PAGE with ethidium bromide post staining is often an easy and informative technique for characterizing the binding affinities and specificities of PNA oligomers. Typically, multiple RNA hairpins or duplexes with single base pair mutations can be used to characterize PNA binding properties, such as binding affinities and specificities. 2-Aminopurine is an isomer of adenine (6-aminopurine); the 2-aminopurine fluorescence intensity is sensitive to local structural environment changes, and is suitable for the monitoring of triplex formation with the 2-aminopurine residue incorporated near the PNA binding site. 2-Aminopurine fluorescence titration can also be used to confirm the binding selectivity of modified PNAs towards targeted double-stranded RNAs (dsRNAs) over single-stranded RNAs (ssRNAs). UV-absorbance-detected thermal melting experiments allow the measurement of the thermal stability of PNA-RNA duplexes and PNA·RNA2 triplexes. Here, we describe the synthesis and purification of PNA oligomers incorporating modified residues, and describe biochemical and biophysical methods for characterization of the recognition of RNA duplexes by the modified PNAs.

Chemomechanical, morphological, and rheological studies of chitosan‐graft‐lactic acid oligomer reinforced poly(lactic acid) bionanocomposite films

ABSTRACTVarious compositions of nontoxic biodegradable poly(lactic acid) (PLA)/chitosan‐graft‐lactic acid oligomer (CH‐g‐OLLA) bionanocomposite films were fabricated with a solution casting technique by the dispersal of CH‐g‐OLLA copolymer at different amounts (1, 3, and 5 wt %) into the PLA matrix. The filler (CH‐g‐OLLA) was synthesized by an in situ condensation polymerization reaction in a microwave, and the grafting of lactic acid oligomer chains at the C2 position of the chitosan backbone was confirmed by the presence of new peaks at 179.08 and 174.41 ppm in 13C‐NMR analysis. The transparency results show the synergic effect of CH‐g‐OLLA in the form of reduced transparency and excellent blocking capability of UV light. Dynamic mechanical analysis confirmed a reduction in the glass‐transition temperature (up to ∼13 °C) with increasing filler concentration; this signified the improvement in the elongation of bionanocomposite films. The rheological studies showed the viscous behavior of the PLA and PLA–CH‐g‐OLLA bionanocomposite films as the storage modulus values were found to be lower than the loss modulus values over the entire range of angular frequency at 180 °C. Furthermore, a Cole–Cole plot and Han plot described the uniform dispersion of the filler in the PLA matrix, its agglomeration at higher loading, and the structural change between the PLA and PLA–CH‐g‐OLLA bionanocomposite films. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 45546.

Synthesis and Characterization of Microencapsulated Phase Change Materials with Poly(urea-urethane) Shells Containing Cellulose Nanocrystals.

The main objective of this study is to develop microencapsulation technology for thermal energy storage incorporating a phase change material (PCM) in a composite wall shell, which can be used to create a stable environment and allow the PCM to undergo phase change without any outside influence. Surface modification of cellulose nanocrystals (CNCs) was conducted by grafting poly(lactic acid) oligomers and oleic acid to improve the dispersion of nanoparticles in a polymeric shell. A microencapsulated phase change material (methyl laurate) with poly(urea-urethane) (PU) composite shells containing the hydrophobized cellulose nanocrystals (hCNCs) was fabricated using an in situ emulsion interfacial polymerization process. The encapsulation process of the PCMs with subsequent interfacial hCNC-PU to form composite microcapsules as well as their morphology, composition, thermal properties, and release rates was examined in this study. Oil soluble Sudan II dye solution in methyl laurate was used as a model hydrophobic fill, representing other latent fills with low partition coefficients, and their encapsulation efficiency as well as dye release rates were measured spectroscopically in a water medium. The influence of polyol content in the PU polymer matrix of microcapsules was investigated. An increase in polyol contents leads to an increase in the mean size of microcapsules but a decrease in the gel content (degree of cross-linking density) and permeability of their shell structure. The encapsulated PCMs for thermal energy storage demonstrated here exhibited promising performance for possible use in building or paving materials in terms of released heat, desired phase transformation temperature, chemical and physical stability, and concrete durability during placement.

Obstruction of BRAFV600E transcription by complementary PNA oligomers as a means to inhibit BRAF-mutant melanoma growth.

Peptide nucleic acid (PNA) oligomers are DNA mimics, which are capable of binding gene sequences 1000-fold more avidly than complementary native DNA by strand invasion and effectively obstruct transcription. Irreversibly obstructing the transcription or replication of a gene sequence, such as BRAFV600E, offers a potential route to specifically target the cancer cell itself. We have employed PNA oligomers to target BRAFV600E in a sequence-specific complementary manner. These PNAs have been modified by appending configurationally stabilizing cationic peptides in order to improve their cellular delivery and target avidity. Our results indicate that exposure of the melanoma cell lines to a modified PNA-peptide conjugate complementary to BRAFV600E mutation sequence results in a concentration-dependent and time-dependent inhibition of cell growth that is specific for the BRAFV600E-mutant melanoma cell lines with inhibition of mRNA and protein expression. Xenograft mouse trials show increased tumor growth delay and necrosis with the BRAFV600E-complementary PNA-peptide conjugates as compared with the saline and scrambled PNA sequence controls. Similarly, quantitative measurement shows a 2.5-fold decrease in Ki67 and a 3-fold increase in terminal deoxynucleotidyl transferase dUTP nick end labeling expression with this approach. PNA-delivery peptide conjugates represent a novel way to target BRAFV600E and represent a new approach in targeting selective oncogenes that induce tumor growth.

Acetylated pectins in raw and heat processed carrots

Heat processing results in softening of carrots, changing the pectin structure. The effect of heat processing on pectin was studied, showing that the amount of pectin in water soluble solids (WSS) and chelating agent soluble solids (ChSS) increased substantially upon heat processing of the carrots. Pectin in WSS from both unprocessed and heat processed carrot had a degree of methyl-esterification (DM) of ≈60% and a degree of acetylation (DA) of ≈20%. Enzymatic degradation released methyl-esterified galacturonic acid oligomers of degree of polymerisation ≥6 carrying acetyl groups. Mass spectrometry confirmed acetylation in highly methyl-esterified homogalacturonan (HG) regions, next to known rhamnogalacturonan (RG-I) acetylation. ChSS HGs were un-acetylated.RG-I levels of both heat processed carrot WSS and ChSS increased. Digestion of WSS with RG-I degrading enzymes showed that WSS arabinan became more linear upon heat processing resulting in the release of oligosaccharides, while in ChSS galactan became more linear.

Vitamin B12 as a carrier of peptide nucleic acid (PNA) into bacterial cells

Short modified oligonucleotides targeted at bacterial DNA or RNA could serve as antibacterial agents provided that they are efficiently taken up by bacterial cells. However, the uptake of such oligonucleotides is hindered by the bacterial cell wall. To overcome this problem, oligomers have been attached to cell-penetrating peptides, but the efficiency of delivery remains poor. Thus, we have investigated the ability of vitamin B12 to transport peptide nucleic acid (PNA) oligomers into cells of Escherichia coli and Salmonella Typhimurium. Vitamin B12 was covalently linked to a PNA oligomer targeted at the mRNA of a reporter gene expressing Red Fluorescent Protein. Cu-catalyzed 1,3-dipolar cycloaddition was employed for the synthesis of PNA-vitamin B12 conjugates; namely the vitamin B12 azide was reacted with PNA possessing the terminal alkyne group. Different types of linkers and spacers between vitamin B12 and PNA were tested, including a disulfide bond. We found that vitamin B12 transports antisense PNA into E. coli cells more efficiently than the most widely used cell-penetrating peptide (KFF)3K. We also determined that the structure of the linker impacts the antisense effect. The results of this study provide the foundation for developing vitamin B12 as a carrier of PNA oligonucleotides into bacterial cells.

Tung Oil Wood Finishes with Improved Weathering, Durability, and Scratch Performance by Addition of Cellulose Nanocrystals.

The main aim of this study is to verify whether cellulose nanocrystal (CNCs)-reinforced tung oil (TO) composites are effective for wood finishes and offer enhanced mechanical and weathering performance owing to the high strength, stiffness, and barrier properties of CNCs. To achieve even dispersion of CNC particles in a polymeric coating film, surface hydrophobization of the CNCs was carried out by grafting poly(lactic acid) oligomers and oleic acid. These new TO coating formulations contain 0 (controlled sample) to 10 wt % of hydrophobized cellulose nanocrystals (hCNCs). The coating performance (degree of wrinkle, leveling, and instantaneous filling) of the hCNC-TO finishes as well as their coating properties (topography, optical properties, mechanical properties, and gas permeability) were investigated in this study. The influence of the hCNC content in the tung oil composite coatings was examined using scratch/impact resistance tests and oxygen transmission rate (OTR) measurements. An increase in the hCNC content led to an increase in scratch/impact resistance as well as a slight decrease in the color-b change, gloss, surface roughness, and OTR value of their film coatings. The hCNC-TO composites for wood coatings presented here showed enhanced performance for utilization in wood-working processes in terms of desired mechanical properties (scratch and impact resistance), weathering performance (color stability), and easy production without any deterioration in surface gloss and roughness after the addition of hCNC to a TO matrix. The hCNC enhanced coating system is a promising candidate for substantial protection of wood surfaces in demanding settings.

Aromatic thermosetting copolyester nanocomposite foams: High thermal and mechanical performance lightweight structural materials

In this study, we present carbon nanoparticle incorporated high-performance aromatic thermosetting copolyester (ATSP) nanocomposite foams. The ATSP nanocomposite foams were fabricated through a facile solid-state mixing method wherein carboxylic acid and acetoxy-functional group oligomers were initially combined with chemically pristine carbon nanofillers separately, while in powder form. The mixtures were then subjected to a thermal condensation polymerization reaction in which the constituent oligomers formed the ester backbone of the ATSP matrix and advanced the molecular weight while acetic acid was emitted as the by-product, and generated a porous nanocomposite morphology. As compared to a neat ATSP foam, the nanocomposite foams exhibited a reduced coefficient of thermal expansion by 25% to 75 × 10−6 °C−1. Thermal stability temperature at 5% mass loss was increased by 30 °C exceeding 500 °C. Compressive mechanical strength was enhanced two-fold, reaching 16 MPa along with a nearly doubled fracture strain, which ultimately yielded improved material toughness.

Abstract 728: Development and validation of ColoScape™ - a new colorectal cancer mutation detection assay

Abstract Introduction: Colorectal cancer is a highly preventable disease as early detection increases rates of patient survival to near 100%. Herein we report the development and validation of a novel multigene mutation biomarker real-time PCR based assay for qualitative detection of colorectal cancer associated biomarkers that comprise tumor specific mutations in the following genes: APC (Exon 15), KRAS (Exon 2), BRAF (Exon 15) and CTNNB1 (Exon 3) called ColoScapeTM . The assay allows the sensitive detection of the presence or absence of mutations in the targeted regions of the genes interrogated. Methodology: The high sensitivity of this multigene biomarker assay is achieved due to xenonucleic acid (XNA) probe technology. XNA probes are novel backbone modified oligomers having natural nucleoside bases (A,T,C and G) that hybridize by Watson-Crick base pairing to natural DNA and RNA with much higher binding affinity than natural deoxyribonucleic acid oligomers of the same sequence. XNA probes are designed that bind to the selected wild-type sequences at the respective genetic loci in the target genes. These XNA probes have a much higher Tm than the primer annealing temperature and suppress amplification of WT DNA templates and only allow amplification of the target mutant DNA templates in the sample. Both single nucleotide polymorphisms (SNP’s) and insertion/deletions (indels) mutations can be detected. For each of the selected mutation sites primers and FAM-labeled TaqMan hydrolysis probes were designed and tested together with the selected XNA oligomers and analytical assay performance confirmed. An internal PCR control amplicon selected in the Human β-Actin (ACTB) gene was employed utilizing a HEX-labeled TaqMan probe. Performance parameters of the assay were established on DNA of colorectal cancer patients extracted from FFPE as well as reference DNA materials (synthetic and cell line derived DNA). The assay demonstrates high sensitivity and specificity in detection of colon cancer and adenoma samples based on the set of biomarkers involved in colorectal cancer neogenesis and disease progression. Conclusion: The ColoScapeTM Colorectal Cancer Mutation Detection assay is shown to be a sensitive tool intended to facilitate research in colon cancer development, early detection, disease monitoring and therapeutic interventions. Citation Format: Michael J. Powell, Elena Peletskaya, Anne Vallerga, Qing Sun, Larry Pastor, Aiguo Zhang. Development and validation of ColoScape™ - a new colorectal cancer mutation detection assay [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 728. doi:10.1158/1538-7445.AM2017-728

Solubilization of prothionamide with micelles of an amphiphilic acrylic acid oligomer with thiohexyl terminal groups and preparation of postoperative cavity filling formulations

An amphiphilic oligomer was prepared by telomerization of acrylic acid in the presence of n-hexyl mercaptan. The structure, molecular weight, critical micelle concentration, and ζ-potential of the oligomer, and also its particle-size distribution in aqueous solution were determined. The product allows solubilization of prothiondamide antituberculosis drug. A procedure was suggested for preparing a filling formulation containing prothionamide for filling postoperative cavities in connective tissue.

Polyimide aerogels crosslinked through cyclic ladder‐like and cage polyamine functionalized polysilsesquioxanes

ABSTRACTPolyimide (PI) aerogels with high porosity, low thermal conductivity, flexibility, low density, and excellent mechanical properties have attracted attention. However, the effect of crosslinker on structures and properties has not been investigated. Preparation of non‐shrinkable, aerogels with excellent performance is still a challenge. A series of PI aerogels are prepared through the polyamic acid oligomer reacting with different crosslinking agents: 1,3,5‐triaminophenoxybenzene (TAB), caged octa(aminophenyl) silsesquioxane, and cyclic ladder‐like poly(aminophenyl) silsesquioxanes. The shrinkage, density, porosity, and compression measurements of the PI aerogels indicate that the PI–polyhedral oligomeric silsesquioxanes (POSS) aerogels show more stable and stronger structures than with the TAB. The physical properties reveal that the introduction of POSS brings more compact and stable crosslinking network structures. The thermal properties of the PI aerogels are tested by dynamic mechanical analysis, thermal gravimetric analysis, and Transient Hot Wire method. The PI–POSS aerogels showed much better thermal stability, lower thermal conductivities, and better thermal insulation. Stable inorganic cores and rigid molecular structures of POSS result in strong mechanical properties, high thermal stability, and low thermal conductivities of the PI aerogels which may have important application in thermal protection against high temperature. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45296.

Efficacy and tolerability of an antiaging dermocosmetic cream containing retinaldehyde 0.05%, ascophyscient, and hyaluronic acid oligomers

Efficacy and tolerability of an antiaging dermocosmetic cream containing retinaldehyde 0.05%, ascophyscient, and hyaluronic acid oligomers